Case Report: A Chinese Family of Type A Insulin Resistance Syndrome With Diabetes Mellitus, With a Novel Heterozygous Missense Mutation of the Insulin Receptor Gene

Type A Insulin resistance syndrome (TAIRS) is an autosomal dominant or recessive genetic disorder caused by insulin dysfunction resulting from insulin receptor (INSR) gene mutation. The main features of TAIRS include hyperinsulinemia, abnormal glucose metabolism, and changes in acanthosis nigricans....

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Detalles Bibliográficos
Autores principales: You, Wei, Yang, Jianming, Wang, Lu, Liu, Yanqun, Wang, Wen, Zhu, Li, Wang, Wei, Yang, Jun, Chen, Fangyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134870/
https://www.ncbi.nlm.nih.gov/pubmed/35634501
http://dx.doi.org/10.3389/fendo.2022.895424

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134870/
https://www.ncbi.nlm.nih.gov/pubmed/35634501
http://dx.doi.org/10.3389/fendo.2022.895424

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